| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32934 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:32773780-32775620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | + | 6.97 | | RFX1 | MA0509.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | - | 6.97 | | RFX2 | MA0600.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | + | 7.18 | | RFX2 | MA0600.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | - | 7.21 | | RFX5 | MA0510.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | + | 7.32 | | RFX5 | MA0510.2 | chr22:32774171-32774187 | AGTTACCATGGCAACT | - | 7.38 | | Znf423 | MA0116.1 | chr22:32774571-32774586 | GCCCCCCAAGGTTGA | + | 6.38 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAATGAGGGC CTGAGGCCAG CAAACCTCTC TGTGGAGCGT GAGAGGGTGA AGGCGAGGCT 60
CCACCATTGC TGGAAAAACA CCATGCCTGC TCTGGGGAAG TTGGGGGATG TTGATTTCAT 120
GGATGTGACT TTCCTATAGC TGATCCCACT CAGGACCACA GGGACCCCCA TGGGTGATTT 180
TCTCAGAGAC CACAGAAACT ATCTTGTGTT TTCTCCTCTC ATACCTTACC ATTGGAGCTT 240
TTCAACAGTC CAGGTGGCGG GGAGGGTTGT GGGACATCAG GGAGTAGGAA CTCCGCAACC 300
TGTGCATGCA GAATTCCCCT TGTAAAGCTC TTGTTGTGCC CCAGACCCTG AGGTCACCTT 360
CTCCTGCACA AGGGGCAGTA GAGACATTGG GAGTTACCAT GGCAACTGGT GCCATGGACT 420
CTGAGGCAGA GCCACTGTGT TTGTCACCTA GGACAGGGAG GATGGACCTT CAGAGATTTG 480
AGCCTCATTA TCCAGATGCA GGTTTGTCAA TAGAAACCCT CTGTCCACCT CTGGACTCCA 540
GCATTATGGG TAAGGCTGAT TGTCTCTGTC ACATAGCTGA ACACAGCCTC ATAAACAGAA 600
AGAGCTCCTG ATCCATGGAA AAATGGATAA AAATGTTGTC CCTCTCATCT TACCAGAATG 660
TACGTTGGGC CAAATAGTGG CCATGGCACT AGCTGTGTAG GTGGCAGCTG CAGAGCCAGG 720
GGCAGTGGAT GGGCCAGGGG GATACGGCAG GGTGGGTGCT TGTGGGGTCA AGGTAGAAGT 780
GGTGAGTAAT GGCCCCCCAA GGTTGAATGT GTTTTGGTGC CTGGGGCTGG CTGGCCTCCA 840
GGAGGCTGGG GCTGGACTGG AGCTGGAGGT GGCAGGCCTC CAAACTGGAA ACAGTGGTCA 900
AAGGTGGGGA TCTGTGCTGC TGCCCCACAG GGGCCCCAGA TATGGGCTAA GCAGTGGCTC 960
CAGGGTTAGT GGAAAGTTTC AAATTTGGGG TGGGGCCACA GAACCCCAGT GCAGGAAGGT 1020
GGTAGTGTCC TTGGCTGAGG CTGTGCTGCC ACCTAGGGAT GTGGGAAGGG TCTGGAAAGA 1080
TGGAAAGTAG TTCCCACTGG AGCCAGCAGG AGGCCCTAGA ATGAGAGGCT AGGAAAGGGG 1140
AGTGGTGTCC GTGGGGGTGA CAATGGTGTC CACTGGGGAG CCAGTCCTGC AGATGTGCTG 1200
GCTGAGGGCC TGGAACTGGC TGCACATGCA GCGAATGGCT GACCAGGGAG AGAGGGGCCT 1260
TAGGATCCAT GAGGAGAGAG AGGCCCTGAG TGAAGAAGAC AGGAGAATGC ATACACATTT 1320
TTGTTGGGGT TGACTACTTC ATTATGGGGG TGCTGCGAGA CATGAGGAAG GCTGAACTGG 1380
CACCTGCTGC AGCTGTGGCT AAGGCCGTGG GGCAGGCCTC AGATGTCTTG AGCAGCCACC 1440
AGCCTGGGTC AGTGCCCTCT CTTCCTCTCT TTGAAGAGCT AGACTTGTAT CCTTGCTGCC 1500
TCACCCATGA GCATCTCTGT TCCTGGTTTC CTCTCCGAGT ATGCACTGAC TCACTCACCT 1560
CCCTATCTTT ATCTCTGAGA ACTTCGAGAC TTGCCTGTGC TCTGAGCAGT GGCTTTAATG 1620
TTGATGACTT TGTGACCATG TGGTATCAGC AGAAGCCAGG GAATCTTCTC TGGGTTCAAC 1680
TGTACTCCTC AAGTCCACTG TGGGGATTAG AAATCCAGGG GCTTGGCTGG GCACCGTGGC 1740
TCACACCTGT AATCCCAGCA CTTTGGGAAG CCGAGGTGGG TGGATCACAA GGTCAGGAGA 1800
TTGAGACCAT CCTGGCTAAC ACAGTGAAAC CCCATCTCTA 1840
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